A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv601250



Internal ID16041973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29883666..29920722hg38UCSC Ensembl
Innerchr6:29851443..29888499hg19UCSC Ensembl
Innerchr6:29959422..29996478hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3837057
hg1937057
hg1837057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10346n54
Supporting Variantsnssv1051742
Samples
Known GenesHLA-H
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv601250
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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